Evidence map›Paper›PMID 36167831›Full record

ReviewSeminars in immunopathology2023

Beyond direct killing-novel cellular immunotherapeutic strategies to reshape the tumor microenvironment.

Duc Huynh, Pia Winter, Florian Märkl, Stefan Endres, Sebastian Kobold

Abstract readReview
In one paragraph

Review in Seminars in immunopathology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. MDSC: a new potential breakthrough in CAR-T therapy for solid tumors.Cell communication and signaling : CCS · 2024
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. gC1qR: A New Target for Cancer Immunotherapy.Frontiers in immunology · 2023
    Review
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Duc HuynhDepartment of Medicine IV, Center of Integrated Protein Science Munich (CIPS-M) and Division of Clinical Pharmacology, Klinikum der Universität München, LMU Lindwurmstrasse 2a, 80337, Munich, Germany.
Pia WinterDepartment of Medicine IV, Center of Integrated Protein Science Munich (CIPS-M) and Division of Clinical Pharmacology, Klinikum der Universität München, LMU Lindwurmstrasse 2a, 80337, Munich, Germany.
Florian MärklDepartment of Medicine IV, Center of Integrated Protein Science Munich (CIPS-M) and Division of Clinical Pharmacology, Klinikum der Universität München, LMU Lindwurmstrasse 2a, 80337, Munich, Germany.
Stefan EndresDepartment of Medicine IV, Center of Integrated Protein Science Munich (CIPS-M) and Division of Clinical Pharmacology, Klinikum der Universität München, LMU Lindwurmstrasse 2a, 80337, Munich, Germany.
Sebastian KoboldDepartment of Medicine IV, Center of Integrated Protein Science Munich (CIPS-M) and Division of Clinical Pharmacology, Klinikum der Universität München, LMU Lindwurmstrasse 2a, 80337, Munich, Germany. Sebastian.kobold@med.uni-muenchen.de.ORCID http://orcid.org/0000-0002-5612-4673

Funding

European Research Council 756017
6 · The paper itself

Abstract

The clinical use of cellular immunotherapies is gaining momentum and the number of approved indications is steadily increasing. One class of cellular therapies-chimeric antigen receptor (CAR)-modified T cells-has achieved impressive results in distinct blood cancer indications. These existing cellular therapies treating blood cancers face significant relapse rates, and their application beyond hematology has been underwhelming, especially in solid oncology. Major reasons for resistance source largely in the tumor microenvironment (TME). The TME in fact functionally suppresses, restricts, and excludes adoptive immune cells, which limits the efficacy of cellular immunotherapies from the onset. Many promising efforts are ongoing to adapt cellular immunotherapies to address these obstacles, with the aim of reshaping the tumor microenvironment to ameliorate function and to achieve superior efficacy against both hematological and solid malignancies.

Indexed as

NeoplasmsReceptors, Chimeric AntigenHumansImmunotherapyImmunotherapy, AdoptiveNeoplasm Recurrence, LocalTumor MicroenvironmentReceptors, Chimeric AntigenCAR-T cellsCellular immunotherapyCytokineInflammationStromaTumor microenvironment

Identifiers

PMID36167831
PMCPMC10121530

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.